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United States Β· US Β· US:22840-5634_36ac182a-ff48-50a9-e063-6394a90aa917
Rhizopus stolonifer
UNII
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGreer Laboratories, Inc.
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 3
- ndc11228405634210 mL in 1 VIAL, MULTI-DOSE (22840-5634-2)
- ndc11228405634450 mL in 1 VIAL, MULTI-DOSE (22840-5634-4)
- ndc1122840563455 mL in 1 BOTTLE, DROPPER (22840-5634-5)
Annotations
UNII (FDA Substance ID)
FEE198DK4Q
RHIZOPUS STOLONIFER
RxCUI 967721
Raw payload (JSON)
{
"unii": {
"unii": "FEE198DK4Q",
"rxcui": "967721",
"inchikey": null,
"display_name": "RHIZOPUS STOLONIFER",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"productid": "22840-5634_36ac182a-ff48-50a9-e063-6394a90aa917",
"productndc": "22840-5634",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "NON-STANDARDIZED ALLERGENIC",
"substance_name": "RHIZOPUS STOLONIFER",
"proprietary_name": "Rhizopus stolonifer",
"active_ingred_unit": "g/mL",
"application_number": "BLA101833",
"marketing_category": "BLA",
"nonproprietary_name": "Rhizopus stolonifer",
"start_marketing_date": "19810915",
"active_numerator_strength": ".025"
}Access this data programmatically
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